Demonstration of cerebellar atrophy in neuroacanthocytosis of 2 siblings.
نویسندگان
چکیده
SUMMARY Neuroacanthocytosis is a rare hereditary disorder characterized by involuntary choreiform movements and erythrocytic acanthocytosis in the peripheral blood. Clinical manifestations of this disorder resemble those of Huntington disease (HD). Neuroimaging features of neuroacanthocytosis are atrophy and signal intensity change of the striata on MR imaging, as in HD. We report herein the cases of 2 siblings with neuroacanthocytosis showing cerebellar atrophy as well as atrophy and signal intensity changes of striata.
منابع مشابه
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ورودعنوان ژورنال:
- AJNR. American journal of neuroradiology
دوره 30 2 شماره
صفحات -
تاریخ انتشار 2009